Cleared Traditional

K983129 - DISPOSABLE MICROSTAAR INJECTOR (MODEL M...

K983129 is the FDA 510(k) clearance for DISPOSABLE MICROSTAAR INJECTOR (MODEL M... by Staar Surgical Co.. It is a Class 1 Ophthalmic device (product code KYB) cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K983129 · Staar Surgical Co. · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1998
Decision
87d
Days
Class 1
Risk

K983129 is an FDA 510(k) clearance for the DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1). Classified as Lens, Guide, Intraocular (product code KYB), Class I - General Controls.

Submitted by Staar Surgical Co. (Monrovia, US). The FDA issued a Cleared decision on December 4, 1998 after a review of 87 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4300 - the FDA ophthalmic device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Staar Surgical Co. devices

Submission Details

510(k) Number K983129 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 08, 1998
Decision Date December 04, 1998
Days to Decision 87 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
23d faster than avg
Panel avg: 110d · This submission: 87d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KYB Lens, Guide, Intraocular
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4300
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KYB Lens, Guide, Intraocular

All 9
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